3) Chromosome 1
1号染色体
1.
Transcriptional Analysis of Chromosome 1 in Diffuse Large B-Cell Lymphoma;
弥漫大B细胞淋巴瘤1号染色体的基因表达分析
2.
Linkage analysis of susceptibility genes for familial schizophrenia on chromosome 1 in Chinese population;
中国人群中家族性精神分裂症与1号染色体的连锁分析
3.
Objective To explore the molecular genetic relationship between chromosome 1 and quantitative trait loci for familial schizophrenia.
目的 探讨家族性精神分裂症的定量性状位点与 1号染色体的分子遗传学关系。
4) Chromosome 9
9号染色体
1.
Genetic Effect of Pericentric Inversion of Chromosome 9;
9号染色体臂间倒位的遗传效应研究
2.
Genetic polymorphism of 10 STR loci on chromosome 9 and its forensic application in Chinese population;
中国人群9号染色体10个STR基因座的遗传多态性及其在法医学中的应用
3.
To understand the genetic polymorphism of 10 STR loci on chromosome 9 and reveal the difference on the linkage maps of different populations, the author used a set of nine tetranucleotide ?and one tritranucleotide repeat STR markers on chromosome 9 chosen from Genome Data Bank.
18个无关汉族 3代家系共 131份血样采自甘肃省白银地区 ,常规PCR扩增 9号染色体的 10个STR基因座 ,采用非变性聚丙烯酰胺凝胶电泳分析。
5) Chromosome 7
7号染色体
1.
Analysis of Pericentric Inversion of Chromosome 7 Associated with Turner Syndrome in Family;
7号染色体臂间倒位伴Turner综合征家系分析(英文)
6) chromosome 12
12号染色体
1.
Analysis of allele frequencies of 6 short tandem repeat loci on chromosome 12 in patients with Kashing-Beck disease;
大骨节病患者12号染色体6个STR位点基因频率分析
2.
To analyze the genetic polymorphism of 7 STR loci(D12S1718,D12S1675,D12S358,D12S367,D12S1638,D12S1646 and D12S1682) on chromosome 12 in Shaanxi Hans.
分析了中国汉族人群中12号染色体上7个短串联重复序列(short tandem repeat,STR)基因座的多态性。
3.
Object We carry out a study on microsatellite instability ( MSI) and loss of heterozygosity ( LOH )of the 4 sites linked to TEL gene on chromosome 12, in order to find out the correlation between MSI, LOH of TEL gene and the occurrence, progression of children acute lymphoblastic leukemia ( ALL) .
目的 研究12号染色体TEL基因微卫星不稳定性和杂合性缺失,以探讨其与儿童急性淋巴细胞白血病发生、发展的关系以及检测的临床意义。
补充资料：无体
【无体】
（术语）无实之体性也，又无实体也。
（术语）无实之体性也，又无实体也。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条